Ljungberg Kogel Ab

FDA Filings

This page includes the latest FDA filings for Ljungberg Kogel Ab. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number8030929
FEI Number1000631051
NameDaniel Kamm
Owner & OperatorLjungberg & Kogel AB
Contact AddressFagelsangsgatan 10
Helsingborg SE-M Skane lan [SE-12] 25110 SE
Official Correspondent
  • Magnus Alquist
  • 046-42-139860-x
US Agent
Importing Logistics Registration
ImporterMacoPharma
Address3675 Crestwood Pkwy Suite 260
Duluth, GA 30096 UNITED STATES
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address8870 Ravello Ct
Naples, FL 34114 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Daniel Kamm [Ljungberg & Kogel AB]
BIOSEALER CR SERIES2013-06-18
Daniel Kamm [Ljungberg & Kogel AB]
BM3302009-12-02
Daniel Kamm [Ljungberg & Kogel AB]
BM330-XBEE2009-12-02
Daniel Kamm [Ljungberg & Kogel AB]
Biostrip2009-08-19
Daniel Kamm [Ljungberg & Kogel AB]
Quality Mixer1999-07-16
Daniel Kamm [Ljungberg & Kogel AB]
BIOMIXER 3301999-07-16
Daniel Kamm [Ljungberg & Kogel AB]
BIOMIXER 3231999-07-16
Daniel Kamm [Ljungberg & Kogel AB]
Apparatus, Blood Cell Diluting1985-03-21

Related Finance Registrations
NCAGE CodeAJ28NLJUNGBERG AND KOGEL AB
NCAGE CodeS7303LJUNGBERG AND KOGEL AB
CAGE CodeS7303LJUNGBERG AND KOGEL AB
CAGE CodeAJ28NLJUNGBERG AND KOGEL AB
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